ZMP
nrip1b
Ensembl ID:
ZFIN ID:
Description:
RIP140-B [Source:UniProtKB/TrEMBL;Acc:Q1L667]
Human Orthologue:
NRIP1
Human Description:
nuclear receptor interacting protein 1 [Source:HGNC Symbol;Acc:8001]
Mouse Orthologue:
Nrip1
Mouse Description:
nuclear receptor interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1315213]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34964 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7287 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34964
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099799 | Nonsense | 380 | 1000 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 10 (position 39626566)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 38316537 |
GRCz11 | 10 | 38260295 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACTGCAGCAGTCTGTTGCTTCTACTTCTTAACAATCACAACTCCCAA[C/T]AGCAGCTCACCAGAAACGGACACCTAGAGGAAGACTGCGGCATCCTCCCA
Long Flanking Sequence:
GGTCCTCACAAAACTCTGCCCAGCCCACAAGCTCTGAATCAATGTCTTGCACAGAACGACTCAAGGCTGTTGCCAGTATGGTTCGGACAAGATCCAGTCCGGCACCTTCACCCAAACCCAGTGTCGCCTGCAGTCAGCTGGCATTGTTGCTGTCCAGCGAGGCTCATCTTCAGCAATACTCTAGAGAGCAGGCTTTAAAAGCACAATTAACCAGTCGATCAGCAAGTGAGAGGCTAGCTGCTATGGCTACTCAACAAACACAGGATAACAGACCTCCCAGCATGGGACAGCCAACAACCACCCCAGACATGCTAAGCTCCTTAAATGCTCAAAACGGAACAATCCCCCCATTAGTGGTTAACTCCAGCAAAAGCAGCCCTTCCCTTTCCTCACCCTCCACGAGACCCCCTAAAGAGAGACGGCCTTTTGACAGGCACGGTCGACCGCCACAGAACTGCAGCAGTCTGTTGCTTCTACTTCTTAACAATCACAACTCCCAA[C/T]AGCAGCTCACCAGAAACGGACACCTAGAGGAAGACTGCGGCATCCTCCCAAGCTGTGCCTCTTCCTTGCAGTCTGACAGCGAGTACTCCAACCCGGATAACAGCCTGACCAAAGACAGCAGTGATGCTGAGAGCTTGTCCAGCTGTTCCCCCATCGACCTTTCCATGAAAAGCAGAACGTCTTGCCAAAAATTTGAGCCCTGCTATTCCTTGCCCCCCTTGATGGATAAGCTCACAGAGTCTCTCGTAAACAAATGGAAGCCGGAAACTTCTGTGCCAAAGGTCCACGAGGCCGTAGATCTGGATACCAGCCCGGACATAAAATCCCAAGATAAGGTCACTCTAATGCAGTTACTGCTGGACCGCAGAAATAATGAGAAGGTAAACAAAAGTTCAGATCATCCTGGTTTGCGGTCTGATTCAGTAATCAGCTGCTTGACTGCAGGCTCACTTAAACGCATTGGCACACCAGAGGACTCCAGGACACAGAGCCCTCAGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7287
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099799 | Essential Splice Site | 711 | 1000 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 10 (position 39625539)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 38315510 |
GRCz11 | 10 | 38259268 |
KASP Assay ID:
554-4524.1 (used for ordering genotyping assays)
KASP Sequence:
GGCAAGGGTGGNCTCTGCTAAGTGTGACAGCTCAAATGGACCTYCTCTGGA[C/G]CCTAACATCAAAAAGGAGCCAGTAGAAGAGAATCTTCAATCAGACCGCTT
Long Flanking Sequence:
CTCCCCTTCATACTCCTTCCCCTCACCCGTTGCCCAGTCCAGTCCTTTAGATCTCTGCAAGTCTAAAGCTCACTCAAGTGAAAAGATGGAGCCGCCGTTCAGTGCCAGCAAGCTACTGCAGAATTTGGCCCAGAGTGGTATAAAGAACTTGTCACCTTCTCCCCCTCCTTTACACCCTCACAAGTTGACAAGCAAAAGGCAAAGTCCAGTACTTGAGCTTGGAAAGCCCCAGGCCTTCTTGAATAGACTTGTCACTCCAGCCAAACAGAACAGTCCCCCTGTATTGGACGAAGGTTCCCCCAAATGTGAGCAATCACTCTCTTCATCATTGCAGATAGAAAACCTTCTTGAGAAGCGCACAGTACTGCAGCTTCTACTGGGAACAGCCTCCCAAAAGGAAAAAAACAGTGGACACAGAGTCTTAGAAGTTACCTCAAGGGGGATGGAGAAGGCAAGGGTGGCTCTGCTAAGTGTGACAGCTCAAATGGACCTTCTCTGGA[C/G]CCTAACATCAAAAAGGAGCCAGTAGAAGAGAATCTTCAATCAGACCGCTTTAATGATGGGGTGCACCACCTGAGTAGATCATCACAACACTCCCCCATTGCTGAAGTACAGGACACAATCAAATCCGAGCTATGTCCCACAGAAACAGCTGCTAAATTTGGACTTCTCAGCCAGCTTTTGAAACAGCAGAATGCCATATACCATTCGAGCCCACACACAAGGCTTGTCAGGAATGCTGTAAAAGAGGAGCCAATGGATTTTCACAGTCCAATTCCGAAGAAAAGAAAACTGTGCATTGAGTTAGCTGAGCGTCTAAGTAGTGAACTCTGTCAACCGCCTGAAGATGTGACTAGCGACAATCCAGCATCTGGAACACCTGAATTGAAAGGTAGAGGGCTGGAAAAACTAAAGGAAGATAAAGCACTAGGGAGTCCAGGGAACAAAACTCCTCTCTCCAGAGAAAGCCAAGGGTTTAATGTTCTCAAGCAACTTCTCCTGTC
Associated Phenotype:
Not determined